(Q28587488)

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

title

Paroxysmal dyskinesias in the lethargic mouse mutant (English)

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

Calcium channel, voltage-dependent, beta 4 subunit

13 November 2019

main subject

1 reference

GOA release 2020-03-11

1 reference

Zubair Khan

1

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

H A Jinnah

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

language of work or name

English

0 references

publication date

1 September 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

published in

Journal of Neuroscience

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

volume

22

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

issue

18

2 references

31 January 2017

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13 November 2019

page(s)

8193-8200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes

13 November 2019

cites work

1 reference

12 December 2020

Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

1 reference

12 December 2020

Calcium channelopathies in the central nervous system

1 reference

12 December 2020

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

1 reference

12 December 2020

Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells

1 reference

12 December 2020

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

1 reference

12 December 2020

Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a

1 reference

12 December 2020

Utility of the lethargic (lh/lh) mouse model of absence seizures in predicting the effects of lamotrigine, vigabatrin, tiagabine, gabapentin, and topiramate against human absence seizures

1 reference

12 December 2020

Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering

1 reference

12 December 2020

Familial paroxysmal kinesigenic choreoathetosis: an electrophysiologic and genotypic analysis

1 reference

12 December 2020

Paroxysmal dyskinesias: clinical features and classification

1 reference

12 December 2020

Ion channel mutations affecting muscle and brain

1 reference

12 December 2020

Paroxetine treatment of aggression and self-injury in persons with mental retardation

1 reference

12 December 2020

Idiopathic epilepsy and paroxysmal dyskinesia

1 reference

12 December 2020

Calcium channels in neurological disease

1 reference

12 December 2020

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit

1 reference

12 December 2020

Epilepsy or paroxysmal kinesigenic choreoathetosis?

1 reference

12 December 2020

Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice

1 reference

12 December 2020

Altered expression and assembly of N-type calcium channel alpha1B and beta subunits in epileptic lethargic (lh/lh) mouse

1 reference

12 December 2020

L-type calcium channels contribute to the tottering mouse dystonic episodes

1 reference

12 December 2020

Episodic movement disorders as channelopathies

1 reference

12 December 2020

Spontaneous polyspike discharges in an epileptic mutant mouse (tottering)

1 reference

12 December 2020

Paroxysmal kinesigenic choreoathetosis: An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied

1 reference

12 December 2020

Environmental risk factors for multifactorial epilepsy in EL mice.

1 reference

12 December 2020

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

1 reference

12 December 2020

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16

1 reference

12 December 2020

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

1 reference

12 December 2020

A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study

1 reference

12 December 2020

Neural network of structures in which GABAB receptors regulate absence seizures in the lethargic (lh/lh) mouse model

1 reference

12 December 2020

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse

1 reference

12 December 2020

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

1 reference

12 December 2020

CACNA1A mutations: hemiplegic migraine, episodic ataxia type 2, and the others

1 reference

12 December 2020

Decreased (45)Ca(2)(+) uptake in P/Q-type calcium channels in homozygous lethargic (Cacnb4lh) mice is associated with increased beta3 and decreased beta4 calcium channel subunit mRNA expression

1 reference

12 December 2020

Pharmacological profiles of generalized absence seizures in lethargic, stargazer and gamma-hydroxybutyrate-treated model mice

1 reference

12 December 2020

Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol))

1 reference

12 December 2020

Localization of mRNAs of voltage-dependent Ca2+-channels: four subtypes of α1- and β-subunits in developing and mature rat brain

1 reference

12 December 2020

Histo-pathologic observations of the nervous and lymphoid tissues of "lethargic" mutant mice

1 reference

12 December 2020

Experimental studies of "lethargic" mutant mice

1 reference

12 December 2020

Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering

1 reference

12 December 2020

Characterization of the antiabsence effects of SCH 50911, a GABA-B receptor antagonist, in the lethargic mouse, gamma-hydroxybutyrate, and pentylenetetrazole models

1 reference

12 December 2020

10.1523/JNEUROSCI.22-18-08193.2002

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

OpenCitations bibliographic resource ID

13 November 2019

5105703

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12223573%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

5105703